Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs172378
C1QA
0.790 0.240 1 22638945 synonymous variant A/G snv 0.49 0.51 11
rs3824662
GATA3
0.752 0.320 10 8062245 intron variant C/A;T snv 11
rs1391441
TET2-AS1 ; TET2
0.763 0.240 4 105207603 intron variant G/A snv 0.70 11
rs117026326
LOC101926943 ; GTF2I
0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10
rs2647012 0.790 0.320 6 32696681 intergenic variant T/C snv 0.64 7
rs6677604
CFH
0.827 0.200 1 196717788 intron variant G/A snv 0.23 7
rs4958881
TNIP1
0.827 0.280 5 151070675 intron variant T/C snv 0.21 7
rs292001
C1QA
0.807 0.320 1 22638465 intron variant G/A snv 0.54 6
rs1456896 0.882 0.200 7 50264865 upstream gene variant C/T snv 0.67 5
rs10127939
FCGR3A
0.851 0.160 1 161548543 missense variant A/C;T snv 4.3E-02; 5.5E-02 5
rs2298804
FCER1A
0.851 0.240 1 159304102 missense variant A/G;T snv 6.6E-03 4
rs4664308
LOC105373717 ; PLA2R1
0.851 0.160 2 160060986 intron variant A/G snv 0.30 4
rs11981433
PON2
0.882 0.240 7 95425028 intron variant T/C;G snv 4
rs2246614
CDHR5
0.882 0.160 11 619789 missense variant T/G snv 0.63 0.59 3
rs2295415
CREM
0.882 0.160 10 35212510 3 prime UTR variant A/G snv 0.19 3
rs4984
LOC105374794 ; ADD2
0.925 0.160 2 70673271 synonymous variant G/A snv 0.12 0.15 3
rs8091180
NFATC1
1.000 0.160 18 79404243 intron variant G/A snv 0.46 3
rs11203368
PADI4
0.925 0.200 1 17340013 intron variant C/T snv 0.57 3
rs329498
PELI1
0.882 0.200 2 64100410 synonymous variant G/A;C;T snv 8.0E-06; 0.34 3
rs434082
SLC8A1
0.925 0.160 2 40257934 intron variant C/T snv 0.14 3
rs1364989 0.925 0.160 4 54145602 intron variant T/C snv 0.73 2
rs601162 0.925 0.160 9 29632144 upstream gene variant A/C;G;T snv 2
rs6697139 0.925 0.160 1 161690906 intergenic variant G/A;T snv 2
rs7692514 0.925 0.160 4 65276878 intergenic variant G/A;C snv 2
rs7773456 0.925 0.160 6 19823007 intron variant T/G snv 0.35 2